Methanol → HCID 12799944, compound

HRID 2412623Notes

Reaction equation

HRID 2412623 reaction equation
B.[C:2]([C:15]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([O:26][CH3:27])=[O:25])=[CH:21][CH:22]=2)[NH:17][CH:16]=1)(=O)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].C(OCC)(=O)C.CO>O1CCCC1.O>[CH2:2]([C:15]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([O:26][CH3:27])=[O:25])=[CH:21][CH:22]=2)[NH:17][CH:16]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]

Participants

7

Conditions

Temperature
50 °C

Procedure

A solution of borane in tetrahydrofuran (134 ml, of strength 1M) in portions (13×10 ml) was added during 20 minutes to a stirred solution of methyl 3-(n-dodecanoyl)indole-6-carboxylate (19.9 g) in a mixture of dry tetrahydrofuran (330 ml) and dry ethyl acetate (330 ml), the temperature of the reaction being maintained at 50° C. by external warming. The mixture was stirred and refluxed for 1.5 hours and then methanol (330 ml) was added to the refluxing mixture during 10 minutes. The mixture was refluxed for a further 30 minutes and water (50 ml) was added. The mixture was distilled at atmospheric pressure to remove the organic solvents to give a yellow residue. The residue was triturated with water (50 ml) to give a solid, which was collected and washed with water (100 ml). The solid was recrystallised from methanol (100 ml) (with treatment with charcoal) and then from toluene to give methyl 3-(n-dodecyl)-indole-6-carboxylate (10 g), in the form of a white solid, m.p. 85°-89° C.

Workup

  1. temperaturerefluxed for 1.5 hours
  2. temperatureThe mixture was refluxed for a further 30 minutes
  3. distillationThe mixture was distilled at atmospheric pressure
  4. customto remove the organic solvents
  5. customto give a yellow residue
  6. customThe residue was triturated with water (50 ml)
  7. customto give a solid, which
  8. customwas collected
  9. washwashed with water (100 ml)
  10. customThe solid was recrystallised from methanol (100 ml) (with treatment with charcoal)

Sources & evidence

ORD record
ord-fd1e0697e0034b3c93dc7aa7cadb82db
Source dataset
uspto-grants-1985_01
Patent number
US04493843

Reaction notes

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